60601-74-3 Usage
Uses
Used in Organic Synthesis:
2-(Cyclohexylmethyl)pyrrolidine is used as a building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows for the creation of complex molecules with potential applications in different industries.
Used in Asymmetric Organic Reactions:
2-(Cyclohexylmethyl)pyrrolidine is used as a chiral auxiliary to control the stereochemistry of the products in asymmetric organic reactions. This helps in obtaining enantiomerically pure compounds, which are essential in the pharmaceutical industry for the development of effective drugs with minimal side effects.
Used in Medicinal Chemistry:
2-(Cyclohexylmethyl)pyrrolidine has potential applications in the field of medicinal chemistry. Its structure can be modified to create novel drug candidates with improved pharmacological properties, such as increased potency, selectivity, and reduced toxicity.
Used in Drug Development:
2-(Cyclohexylmethyl)pyrrolidine serves as a starting material for the preparation of novel drug candidates. Its versatile chemistry allows for the synthesis of new compounds with potential therapeutic applications in various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 60601-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,0 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60601-74:
(7*6)+(6*0)+(5*6)+(4*0)+(3*1)+(2*7)+(1*4)=93
93 % 10 = 3
So 60601-74-3 is a valid CAS Registry Number.
60601-74-3Relevant academic research and scientific papers
3-(Piperidino-lower-alkyl)-indoles
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, (2008/06/13)
1-Acyl-3-(amino-lower-alkyl)indoles, useful as anti-inflammatory agents, are prepared either by acylation of a 3-(amino-lower-alkyl)indole; by Fisher indole synthesis from an N'-acylphenylhydrazine and an amino-lower-alkanone; by alkylation of an amine with a 1-acyl-3-(halo-lower-alkyl)indole; or by reductive alkylation of a 1-acyl-3-indole-lower-alkylcarboxaldehyde.
Phenyl-lower-alkylamines
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, (2008/06/13)
Phenyl-lower-alkylamines having anti-inflammatory activity are prepared either by reductive alkylation of an amine with a phenyl-lower-alkanaldehyde; by condensation of a phenyl-lower-alkanaldehyde with a secondary amine, conversion of the resulting phenylvinylamine to the corresponding iminium salt, and reduction of the latter with an alkali metal borohydride; or by reaction of a phenyl-lower-alkanoyl halide with an amine and reduction of the resulting amide with a reagent effective to reduce an amide to an amine.
